Home Canadian DIN search TENECTEPLASE DIN 02562804
TNKASE DIN 02562804
Status: Marketed
Holder: HOFFMANN-LA ROCHE LIMITED
Health Canada record
Active ingredient(s) TENECTEPLASE 25 MG Dosage form Powder For Solution Route Intravenous Schedule PRESCRIPTION; SCHEDULE D Class Human ATC B01AD11 TENECTEPLASE Original market date 13-Aug-2026 Current status date 13-Aug-2026 Source Health Canada DPD
Establishment licence of the holder Hoffmann-La Roche Limited — licence 100006, currently licensed, last inspection rating C (2024-06-25).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing TENECTEPLASE DIN Product Company Form Strength Status 02244826 TNKASE HOFFMANN-LA ROCHE LIMITED Powder For Solution TENECTEPLASE 50 MG Marketed
Notices of Compliance NOC Date Submission Reason 36366 2025-11-13 Supplement to a New Drug Submission (SNDS) New indication :
Intravenous use in adults for the treatment of acute ischemic
stroke (AIS). Treatment is to be initiated within 4.5 hours from
the onset of AIS symptoms and after exclusion of intracranial
haemorrhage.
New strength
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